1 / 26

Obtaining Specimens for Microbiological Evaluation

Obtaining Specimens for Microbiological Evaluation. IPM-2. Bacteremia I. Most bacteremias are intermittent One blood culture is rarely sufficient Staphylococcus epidermidis Frequent contaminant Commonest cause of PVE Two blood cultures usually sufficient

ostinmannual
Télécharger la présentation

Obtaining Specimens for Microbiological Evaluation

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Obtaining Specimens for Microbiological Evaluation IPM-2

  2. Bacteremia I • Most bacteremias are intermittent • One blood culture is rarely sufficient • Staphylococcus epidermidis • Frequent contaminant • Commonest cause of PVE • Two blood cultures usually sufficient • Three or four if suspect likely contaminant • Antibiotic therapy

  3. Blood Cultures - Volume The magnitude of bacteremia may be low (<1cfu/ml) Higher volumes have higher yield

  4. Blood Cultures - Lab Aspects • Additives (SPS, resins) increase yield • Aerobic and anaerobic bottle = onebloodculture • Five days incubation sufficient • Exception: Brucella, Histoplasma, Mycobacterium, Bartonella, Legionella • Automated Systems detect CO2 • Subculture detected bottles

  5. Aerobic/Anaerobic Blood Culture Bottles

  6. AFB Blood Culture Bottle

  7. Obtaining Blood Culture • Locate the vein • Prep kit • Alcohol 5 sec. Dry 30-60 sec • Tincture of Iodine-center to periphery. Dry 45-60 sec • Remove caps, clean with alcohol • Put on gloves • Without palpating, draw 20 ml and put 10 in anaerobic and 10 in aerobic bottle • Dispose of syringe in sharps container • Label bottles and send to lab

  8. Blood Culture Prep Kit

  9. Sputum Culture Reliability • Expectorated unreliable because of contamination • Reliability  if physician observes • Laboratory reliability screen • > 25 PMN’s, < 10 oral squamous cells per hpf

  10. Sputum Container

  11. Sputum • Gram stain • Useful for immediate therapy • May be more reliable than culture • Many PMN’s with single bacterial morphology • AFB - first morning specimen • Pneumocystis carinii - induced specimen

  12. Nasal Cultures • Virus • Use wire swab • Place in nose 1-3 cm, rotate, 10-15 sec • Obtain viral transport medium from lab • Bacterial • Culturette with rigid or wire swab • Suspect pertussis - special media

  13. Wire Swab

  14. Throat Cultures • For Group A strept, diphtheria, gonorrhea • Tongue blade - visualize pharynx and tonsils • Rub swab over tonsils and pharynx • INCLUDE ANY EXUDATE • Insert into holder, crush vial

  15. Swabs for Bacterial (red) and Viral (green) Cultures

  16. Cerebrospinal Fluid • Use sterile technique • First or second tube to Microbiology • Studies • Gram stain - one drop cloudy fluid or sediment • Aerobic culture - 1.0 ml • Viral culture - 1.0 ml • AFB or fungal culture - up to 10 ml

  17. Wounds: General Principles • Closed space infections provide reliable specimens • Open wounds heavily contaminated • May quantitate • May obtain culture by aspirating advancing border • Culture skin, soft tissue or wound abscesses for anaerobic and aerobic organisms • Transport in capped syringe or special tube

  18. Wound Culture • Closed space abscesses • Decontaminate skin • Insert needle and aspirate or aspirate pus after incision • Open wound • Remove superficial exudate • Aspirate through margin or swab (least reliable) • Transport • Capped syringe or anaerobic transport tube • Rapidly to lab

  19. Urine - General • Collection method must avoid contamination • Clean catch, midstream voided • Catheterized urine • Suprapubic aspiration • Cultures performed quantitatively • Less than 10,000 per ml suggest contamination

  20. Clean Catch, Midstream Urine • Cleanse periurethral area with soap and water • Pass initial urine into toilet, then collect specimen in cup • Instructionstopatientarecritical

  21. Instructions for Patient • Remove underpants completely so they will not get soiled. • Sit comfortably on the seat, but do not leave your knees in front of you. Instead swing one knee to the side as far as you can. • Spread yourself with one hand, and continue to hold yourself spread while you clean and collect the specimen. • Wash—Be sure you wash well and rinse well before you collect your urine sample. Wash only the area from which you pass urine. You do not have to wash hard, but wash slowly. Be sure to wipe from the front of your body towards the back. Wash between the folds of skin as carefully as you can. • Do not put sponges in the toilet. Put them back in the plate. • Rinse—After you have washed with each soap pad, rinse with each moistened pad with the same front to back motion. Do not use any pad more than once. • Hold cup by the outside and pass your urine into the cup. If you touch the inside of the cup or drop it on the floor, ask the nurse to give you a new one.

  22. Catheterized Urine • Cleanse periurethral area with soap and water • DO NOT RECONTAMINATE • Insert catheter into bladder • Discard initial urine • Collect specimen in sterile cup • Chronic indwelling Foley catheter • Clamp tubing below junction (or port) • Disinfect with alcohol • Insert needle (on syringe) through port or catheter wall and aspirate

  23. Suprapubic Aspiration • BE CERTAIN BLADDER IS FULL - PALPATE OR PERCUSS • Prep skin with alcohol or iodine • Anesthetize with lidocaine • Introduce needle 2.0 cm above symphysis • Aspirate 20 ml for culture

  24. Suprapubic Aspiration

  25. Wire Swab

  26. IV Start Kit

More Related